Regional and cellular gene expression changes in human Huntington's disease brain.
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The palmitoyl acyltransferase HIP14 shares a high proportion of interactors with huntingtin: implications for a role in the pathogenesis of Huntington's diseaseGenome-wide siRNA screen reveals amino acid starvation-induced autophagy requires SCOC and WACTherapeutic potential of mood stabilizers lithium and valproic acid: beyond bipolar disorderThe HDAC inhibitor 4b ameliorates the disease phenotype and transcriptional abnormalities in Huntington's disease transgenic mice.Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaModeling Huntington's disease with induced pluripotent stem cellsPossible involvement of self-defense mechanisms in the preferential vulnerability of the striatum in Huntington's diseaseGenetics and neuropathology of Huntington's diseaseTranscriptional dysregulation in Huntington's disease: a failure of adaptive transcriptional homeostasisN17 Modifies mutant Huntingtin nuclear pathogenesis and severity of disease in HD BAC transgenic miceReinstating aberrant mTORC1 activity in Huntington's disease mice improves disease phenotypes.The Wnt receptor Ryk reduces neuronal and cell survival capacity by repressing FOXO activity during the early phases of mutant huntingtin pathogenicityAAV-dominant negative tumor necrosis factor (DN-TNF) gene transfer to the striatum does not rescue medium spiny neurons in the YAC128 mouse model of Huntington's diseaseMaintenance of basal levels of autophagy in Huntington's disease mouse models displaying metabolic dysfunctionDoes neuroinflammation fan the flame in neurodegenerative diseases?RNA-mediated pathogenic mechanisms in polyglutamine diseases and amyotrophic lateral sclerosisStriatal-enriched protein tyrosine phosphatase expression and activity in Huntington's disease: a STEP in the resistance to excitotoxicityStructure, binding interface and hydrophobic transitions of Ca2+-loaded calbindin-D(28K)A chaperome subnetwork safeguards proteostasis in aging and neurodegenerative diseaseHuman accelerated region 1 noncoding RNA is repressed by REST in Huntington's diseaseThe bifunctional microRNA miR-9/miR-9* regulates REST and CoREST and is downregulated in Huntington's diseaseCRNDE: A Long Non-Coding RNA Involved in CanceR, Neurobiology, and DEvelopmentUnbiased gene expression analysis implicates the huntingtin polyglutamine tract in extra-mitochondrial energy metabolismDEGAS: de novo discovery of dysregulated pathways in human diseasesDecreased striatal RGS2 expression is neuroprotective in Huntington's disease (HD) and exemplifies a compensatory aspect of HD-induced gene regulationFunctional roles for the striatal-enriched transcription factor, Bcl11b, in the control of striatal gene expression and transcriptional dysregulation in Huntington's diseaseAn evolutionarily conserved long noncoding RNA TUNA controls pluripotency and neural lineage commitmentGenome-wide loss of 5-hmC is a novel epigenetic feature of Huntington's diseaseNanopublications for exposing experimental data in the life-sciences: a Huntington's Disease case studyHuntington’s disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer’s diseaseImprovement of neuropathology and transcriptional deficits in CAG 140 knock-in mice supports a beneficial effect of dietary curcumin in Huntington's disease.A novel method for fast Change-Point detection on simulated time series and electrocardiogram dataMice lacking caspase-2 are protected from behavioral changes, but not pathology, in the YAC128 model of Huntington disease.Expression analysis of novel striatal-enriched genes in Huntington disease.Assessment of the relationship between pre-chip and post-chip quality measures for Affymetrix GeneChip expression data.Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood.Alterations in cortical excitation and inhibition in genetic mouse models of Huntington's disease.Transgenic mice expressing caspase-6-derived N-terminal fragments of mutant huntingtin develop neurologic abnormalities with predominant cytoplasmic inclusion pathology composed largely of a smaller proteolytic derivative.Longitudinal transcriptomic dysregulation in the peripheral blood of transgenic Huntington's disease monkeys.Molecular networks involved in mouse cerebral corticogenesis and spatio-temporal regulation of Sox4 and Sox11 novel antisense transcripts revealed by transcriptome profiling.
P2860
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P2860
Regional and cellular gene expression changes in human Huntington's disease brain.
description
2006 nî lūn-bûn
@nan
2006 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Regional and cellular gene expression changes in human Huntington's disease brain.
@ast
Regional and cellular gene expression changes in human Huntington's disease brain.
@en
type
label
Regional and cellular gene expression changes in human Huntington's disease brain.
@ast
Regional and cellular gene expression changes in human Huntington's disease brain.
@en
prefLabel
Regional and cellular gene expression changes in human Huntington's disease brain.
@ast
Regional and cellular gene expression changes in human Huntington's disease brain.
@en
P2093
P50
P356
P1476
Regional and cellular gene expression changes in human Huntington's disease brain.
@en
P2093
Aaron K Aragaki
Alexandre Kuhn
Andrew D Strand
Anne B Young
Beth Synek
Cathy Hartog
Darlene R Goldstein
Francois Collin
Gareth Hughes
P304
P356
10.1093/HMG/DDL013
P577
2006-02-08T00:00:00Z